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Preparation et reactivite du derive lithie issu du dioxolanne du -ceto pentanoate de trimethylsilyle.

✍ Scribed by Jean Louis Moreau; René Couffignal


Book ID
104219826
Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
203 KB
Volume
23
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


The organolithium reagent $ issued from trimethylsilyl 4,4_ethylendioxypentanoate 2 reacts with ketones ; it affords 8-hydroxy-acids 1 and B-ethylenic ketones 8. This reaction is an efficient route for carbonyl olefination. 4 also acts towards mixed carboxylic and carbonic anhydrides as a homoenolate equivalent.

Nous avons rdcemment signale' que le dioxolanne acide 2 dtait facilement accessible -


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